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(Senior) QA Qualification Specialist(m/w/x)
QA qualification for pharmaceutical projects, compiling and releasing documents at a global life sciences firm. Significant pharmaceutical industry experience with cGMP regulations understanding required. Project-based work, agile career path.
Anforderungen
- Academic degree in Engineering, Chemistry, Biotechnology, or related field, or vocational education with strong relevant experience
- Significant experience in the pharmaceutical industry, ideally in a QA role
- Good understanding of applicable cGMP regulations
- General knowledge of engineering and manufacturing processes
- Ability to oversee project execution to identify non-compliance from quality standards
- Fluent German (written and verbal) required; good English language skills advantageous
Aufgaben
- Represent QA Qualification in project organizations
- Coordinate QA interests during project phases
- Drive implementation of new qualification strategies
- Compile, review, and release Qualification Documents
- Support and approve quality risk analyses
- Perform assessments and approvals of technical change requests
- Represent qualification topics during customer audits
- Drive CAPA and Effectiveness Checks to completion
- Ensure deviations are investigated and recorded
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – Grundkenntnisse
Benefits
Boni & Prämien
- Compensation programs recognizing high performance
Mitarbeiterrabatte
- Numerous lifestyle benefits
- Leisure benefits
Familienfreundlichkeit
- Family benefits
Karriere- und Weiterentwicklung
- Agile career
Lockere Unternehmenskultur
- Dynamic work culture
- Inclusive workplace
Sinnstiftende Arbeit
- Ethical workplace
Sonstige Vorteile
- Relocation assistance
Noch nicht perfekt?
- CH12 Lonza AGVollzeitnur vor OrtSeniorVisp
- Lonza
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(Senior) QA Qualification Specialist(m/w/x)
QA qualification for pharmaceutical projects, compiling and releasing documents at a global life sciences firm. Significant pharmaceutical industry experience with cGMP regulations understanding required. Project-based work, agile career path.
Anforderungen
- Academic degree in Engineering, Chemistry, Biotechnology, or related field, or vocational education with strong relevant experience
- Significant experience in the pharmaceutical industry, ideally in a QA role
- Good understanding of applicable cGMP regulations
- General knowledge of engineering and manufacturing processes
- Ability to oversee project execution to identify non-compliance from quality standards
- Fluent German (written and verbal) required; good English language skills advantageous
Aufgaben
- Represent QA Qualification in project organizations
- Coordinate QA interests during project phases
- Drive implementation of new qualification strategies
- Compile, review, and release Qualification Documents
- Support and approve quality risk analyses
- Perform assessments and approvals of technical change requests
- Represent qualification topics during customer audits
- Drive CAPA and Effectiveness Checks to completion
- Ensure deviations are investigated and recorded
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – Grundkenntnisse
Benefits
Boni & Prämien
- Compensation programs recognizing high performance
Mitarbeiterrabatte
- Numerous lifestyle benefits
- Leisure benefits
Familienfreundlichkeit
- Family benefits
Karriere- und Weiterentwicklung
- Agile career
Lockere Unternehmenskultur
- Dynamic work culture
- Inclusive workplace
Sinnstiftende Arbeit
- Ethical workplace
Sonstige Vorteile
- Relocation assistance
Über das Unternehmen
CH12 Lonza AG
Branche
Pharmaceuticals
Beschreibung
The company is a global leader in life sciences, dedicated to improving lives through innovative solutions.
Noch nicht perfekt?
- CH12 Lonza AG
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